Canonical Allele Identifier: CA1330502576

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222201930A= , CM000664.2:g.222201930A=	GRCh38
NC_000002.11:g.223066649A= , CM000664.1:g.223066649A=	GRCh37
NC_000002.10:g.222774893A=	NCBI36
NG_011632.1:g.102052T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.1174-488T=	ENSP00000338767.5:n.1174-488T=
ENST00000344493.9:c.1174-488T=	ENSP00000342092.4:n.1174-488T=
ENST00000350526.9:c.1434T=	ENSP00000343052.4:p.Thr478=
ENST00000392070.7:c.1420+14T= MANE Select	ENSP00000375922.3:n.1420+14T=
ENST00000464706.6:n.858+14T=
ENST00000644699.1:n.746+14T=
ENST00000646154.1:n.1234+14T=
ENST00000336840.10:c.1174-488T=	ENSP00000338767.5:n.1174-488T=
ENST00000344493.8:c.1174-488T=	ENSP00000342092.4:n.1174-488T=
ENST00000350526.8:c.1434T=	ENSP00000343052.4:p.Thr478=
ENST00000392069.6:c.1420+14T=	ENSP00000375921.2:n.1420+14T=
ENST00000392070.6:c.1420+14T=	ENSP00000375922.2:n.1420+14T=
ENST00000409551.7:c.1417+14T=	ENSP00000386750.3:n.1417+14T=
NM_001127366.2:c.1417+14T=	NP_001120838.1:n.1417+14T=
NM_181457.3:c.1434T=	NP_852122.1:p.Thr478=
NM_181458.3:c.1420+14T=	NP_852123.1:n.1420+14T=
NM_181459.3:c.1420+14T=	NP_852124.1:n.1420+14T=
NM_181460.3:c.1174-488T=	NP_852125.1:n.1174-488T=
NM_181461.3:c.1174-488T=	NP_852126.1:n.1174-488T=
XM_011511278.1:c.1564+14T=	XP_011509580.1:n.1564+14T=
XM_011511279.1:c.856+14T=	XP_011509581.1:n.856+14T=
NM_001127366.3:c.1417+14T=	NP_001120838.1:n.1417+14T=
NM_181457.4:c.1434T=	NP_852122.1:p.Thr478=
NM_181458.4:c.1420+14T= MANE Select	NP_852123.1:n.1420+14T=
NM_181459.4:c.1420+14T=	NP_852124.1:n.1420+14T=
NM_181460.4:c.1174-488T=	NP_852125.1:n.1174-488T=
NM_181461.4:c.1174-488T=	NP_852126.1:n.1174-488T=